Senior CRC
Accellacare, Hickory, NC, United States
Sr Clinical Research Coordinator
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Accellacare , part of ICON's clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.
Title:
Sr Clinical Research Coordinator
Location:
221 13th Avenue Place NW, Suite 201, Hickory, Raleigh, North Carolina 27609
Summary:
The Sr CRC ensures the safety of our participants, promotes the mission of Accellacare, and consistently strives to meet and exceed priorities discussed with supervisor. The Sr CRC will actively recruit and promote our service to suitable participants and sponsor representatives. Additionally, the Sr CRC will autonomously perform tasks required to coordinate and complete multiple studies according to the protocol. They will assist the Manager of Clinical Operations and Sr. Clinical Research Coordinators with staff development through mentoring and site-level quality assurance.
Duties
Performs study start-up duties including the production of a recruitment tool and progress notes, as well as phone screening patients and identifying participants for trials on site
Proactively develops and executes recruitment plans that meet and exceed enrollment goals
Performs study start-up duties including the production of a recruitment plan, recruitment tool, and progress notes, as well as phone screening participants
Completes training on Clinical Trial Management System and maintains proper skills to update database, complete participant reimbursement, capture referral source of participants, and create calls lists to promote recruitment
Attends investigator meetings
Creates and updates source documents/progress notes and utilizes templates provided in the Core Operating Guidelines
Accurately collects study data via source documents/progress notes as required by the protocol
Performs technical requirements of the study protocol, including lab work (phlebotomy and processing), blood pressure, electrocardiograms, Holter monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, or any procedure necessary for the protocol as ordered by the investigator or specified by a protocol
Continuously reviews inclusion and exclusion criteria for each participant during the trial
Documents laboratory data and adverse reactions, presents this information to an investigator in a timely manner, and immediately notifies investigators, the Institutional Review Board and sponsor of any serious adverse events
Builds and maintains strong relationships with Investigators and provides ongoing communication about trial status and participants
Dispenses study medication at the direction of the Investigator
Maintains communication with the monitor from the sponsoring company through telephone contact, written communication, and on-site visits
Enters visit data in the Electronic Data Capture (EDC) or Case Report Forms (CRF) within timelines provided by sponsor
To Be Successful, You Will Have
Bachelor's Degree
3+ years of experience as a clinical research coordinator or equivalent role
High attention to detail
Interest in a clinical research career
What ICON Can Offer You
Our success depends on the quality of our people. We’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to a competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance for you and your family.
Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of professionals
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion and belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process or to perform the essential functions of a position, please let us know or submit a request here.
If you are interested in the role but aren’t sure you meet all requirements, we encourage you to apply anyway—there’s every chance you’re exactly what we’re looking for at ICON for this or other roles.
If you are a current ICON employee, please click here to apply.
#J-18808-Ljbffr
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Accellacare , part of ICON's clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.
Title:
Sr Clinical Research Coordinator
Location:
221 13th Avenue Place NW, Suite 201, Hickory, Raleigh, North Carolina 27609
Summary:
The Sr CRC ensures the safety of our participants, promotes the mission of Accellacare, and consistently strives to meet and exceed priorities discussed with supervisor. The Sr CRC will actively recruit and promote our service to suitable participants and sponsor representatives. Additionally, the Sr CRC will autonomously perform tasks required to coordinate and complete multiple studies according to the protocol. They will assist the Manager of Clinical Operations and Sr. Clinical Research Coordinators with staff development through mentoring and site-level quality assurance.
Duties
Performs study start-up duties including the production of a recruitment tool and progress notes, as well as phone screening patients and identifying participants for trials on site
Proactively develops and executes recruitment plans that meet and exceed enrollment goals
Performs study start-up duties including the production of a recruitment plan, recruitment tool, and progress notes, as well as phone screening participants
Completes training on Clinical Trial Management System and maintains proper skills to update database, complete participant reimbursement, capture referral source of participants, and create calls lists to promote recruitment
Attends investigator meetings
Creates and updates source documents/progress notes and utilizes templates provided in the Core Operating Guidelines
Accurately collects study data via source documents/progress notes as required by the protocol
Performs technical requirements of the study protocol, including lab work (phlebotomy and processing), blood pressure, electrocardiograms, Holter monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, or any procedure necessary for the protocol as ordered by the investigator or specified by a protocol
Continuously reviews inclusion and exclusion criteria for each participant during the trial
Documents laboratory data and adverse reactions, presents this information to an investigator in a timely manner, and immediately notifies investigators, the Institutional Review Board and sponsor of any serious adverse events
Builds and maintains strong relationships with Investigators and provides ongoing communication about trial status and participants
Dispenses study medication at the direction of the Investigator
Maintains communication with the monitor from the sponsoring company through telephone contact, written communication, and on-site visits
Enters visit data in the Electronic Data Capture (EDC) or Case Report Forms (CRF) within timelines provided by sponsor
To Be Successful, You Will Have
Bachelor's Degree
3+ years of experience as a clinical research coordinator or equivalent role
High attention to detail
Interest in a clinical research career
What ICON Can Offer You
Our success depends on the quality of our people. We’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to a competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance for you and your family.
Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of professionals
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion and belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process or to perform the essential functions of a position, please let us know or submit a request here.
If you are interested in the role but aren’t sure you meet all requirements, we encourage you to apply anyway—there’s every chance you’re exactly what we’re looking for at ICON for this or other roles.
If you are a current ICON employee, please click here to apply.
#J-18808-Ljbffr